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Laparoscopic Surgical Procedures clinical trials

View clinical trials related to Laparoscopic Surgical Procedures.

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NCT ID: NCT03704259 Completed - Clinical trials for Laparoscopic Surgical Procedures

Nano-Ceramic Coating for Laparoscope Lens

Start date: September 1, 2018
Phase:
Study type: Observational

The investigator tests the effectiveness of nano-ceramic coating when applied (painted) on laparoscope lens to protect it from fogging or smearing during laparoscopic operations

NCT ID: NCT03503929 Enrolling by invitation - Clinical trials for Laparoscopic Surgical Procedures

Feasibility and Usability of LaparoGuard

Start date: June 21, 2019
Phase: N/A
Study type: Interventional

LaparoGuard is intended as an adjunctive safety system for laparoscopic surgery. The system allows surgeons to virtually annotate a safe anatomical volume inside the body cavity of the patient during a laparoscopic surgery. The surgeon then receives notification throughout the procedure whenever a tracked rigid instrument has exited that volume. This open label, prospective, feasibility, single site, multi-investigator trial will evaluate the feasibility and usability of the LaparoGuard system during laparoscopic surgical procedures.

NCT ID: NCT02756052 Completed - Clinical trials for Laparoscopic Surgical Procedures

Enhancing Laparoscopic Skill Acquisition and Retention With Transcranial Direct-current Stimulation

Start date: March 2016
Phase: N/A
Study type: Interventional

Recent changes in medical training environments and restrictive work-hour regulations have greatly impacted trainees, limiting the number of opportunities to gain proficiency in procedural skills. Reports suggest that medical residents lack confidence in their ability to perform certain medical procedures, and program directors often do not believe their residents can operate independently in major procedures. Simulator based task training (SBTT) has provided a safe and ethically appropriate method of skill acquisition but training opportunities remain limited. Methods to enhance motor learning during these training opportunities have not been described. Transcranial direct-current stimulation (tDCS) is an emerging form of non-invasive brain stimulation that has been shown to improve motor learning. tDCS has been shown to enhance increasingly complex skill acquisition. The investigators propose to examine if tDCS can improve the acquisition and retention of laparoscopic surgical skill. The investigators propose a double blind, sham-controlled randomized trial applying tDCS during evidence-based SBTT of medical students and surgical residents, to determine if brain stimulation can enhance training effects and long-term skill acquisition. Even a modest enhancement carries the potential to transform medicosurgical skills training.

NCT ID: NCT02417857 Completed - Clinical trials for Laparoscopic Surgical Procedures

Comparison of Single İncision Laparoscopic Cholecystectomy Versus Laparoscopic Cholecystectomy

Start date: January 2011
Phase: N/A
Study type: Interventional

The aim of this study is to compare outcomes of quality-of-life measures and evaluate the body image and cosmesis between Single Incision Laparoscopic Cholecystectomy (SILC) and Conventional Laparoscopic Cholecystectomy (CLC).Twenty eight patients underwent SILC and 30 underwent LC.Fifty-eight patients were included the study and divided into two groups. The results of the questionnaires were statistically compared.

NCT ID: NCT02320578 Completed - Clinical trials for Uterine Cervical Neoplasms

2D Versus 3D Radical Laparoscopic Hysterectomy for Cervical Cancer: a Prospective Randomized Trial

Start date: October 2014
Phase: N/A
Study type: Interventional

The aim of this prospective randomized pilot study is to verify if the operative time of a Radical abdominal hysterectomy (LRH) with pelvic lymphadenectomy for early stage cervical cancer (FIGO stages IA2-IB1-IIA<2cm) and for advanced stage cervical cancer (FIGO stages IB2-IIA>2cm-IIB) submitted to neoadjuvant chemotherapy (NACT) with complete clinical response could be further reduced using 3D Laparoscopy (Olympus Medical Systems Corp) versus standard laparoscopy

NCT ID: NCT00433316 Completed - Clinical trials for Laparoscopic Surgical Procedures

Pain Relief by Intra-Peritoneal Ropivacaine During Gynecological Laparoscopy

Start date: February 2007
Phase: Phase 3
Study type: Interventional

In our prospective, randomized, placebo controlled and double-blinded study we will study the efficacy of intraperitoneal ropivacaine nebulization on pain relief during gynecological laparoscopic surgery.

NCT ID: NCT00280553 Recruiting - Clinical trials for Laparoscopic Surgical Procedures

A Pilot Study of Bupivacaine Infusion in Abdominal Surgery

Start date: April 2005
Phase: Phase 2
Study type: Interventional

The incisions used in abdominal surgery can be quite painful, requiring strong pain medications. A new pain pump that trickles small amounts of local freezing into the incision has been developed that helps numb the area so that the patient does not feel the pain for two to five days after surgery. The main research question is whether use of the pain pump will result in decreased hospital length of stay. The research is important because if the pain pump is found to be effective, it can substantially decrease the length of stay. Areas to be studied include hospital length of stay, patient's comfort post-operatively, and post-operative complications.